Oral mucositis and microbial colonization in oral cancer patients undergoing radiotherapy and chemotherapy: A prospective analysis in a tertiary care dental hospital

被引:140
作者
Subramaniam, Nandhini [1 ]
Muthukrishnan, Arvind [1 ]
机构
[1] Saveetha Inst Med & Tech Sci, Saveetha Dent Coll, Dept Oral Med & Radiol, Chennai, Tamil Nadu, India
关键词
antibiotic-resistance genes; facultative anaerobes; gene expression; oral cancer; oral mucositis; NECK-CANCER; MANAGEMENT; AGENTS; FLORA; GENE; HEAD;
D O I
10.1111/jicd.12454
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Aim The ulcerative phase of oral mucositis following radiotherapy/chemotherapy for oral cancer colonizes bacteria, fungi and viruses. The role of a microbiota, specifically bacterial colonization in oral mucositis, is still unclear, and there is no existing data that correlates the shift in the bacterial colonization with mucositis severity. The aim of this study was to assess the bacterial colonization and study the MCR-1 (mobilized colistin resistance), VIM2 (beta-lactam resistance), TET(K) (tetracycline resistance) and bla(KPC) (carbapenem resistance) genes' expression in isolated facultative anaerobes at 3 time points in oral mucositis patients undergoing radiotherapy and concomitant radiochemotherapy. Methods A total of 24 oral cancer patients were divided into 2 groups: A (N = 12) undergoing radiotherapy; and B (N = 12) undergoing radiochemotherapy. Saliva was collected from all patients at 3 time intervals during the treatment. The isolated bacterial colonies were subjected to gene expression and analysis. Results Staphylococcus aureus (22%), Staphylococcus epidermidis (29%), Pseudomonas aeruginosa (28%), Escherichia coli (25%) and Klebsiella pneumoniae (26%) are the facultative anaerobes isolated from saliva. The bacterial isolates obtained during and at the end of therapy appeared to express a higher level of antibiotic-resistance genes (VIM2, MCR-1, TET[K], bla(KPC)) than those isolated at the onset of therapy. Conclusion Bacterial colonization and gene expression varied during different stages of mucositis.
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共 27 条
[1]  
Bagg J, 2009, MICROBIOL ECOL HLTH, V8, P51
[2]   Risk factors for ulcerative oral mucositis in cancer patients: unanswered questions [J].
Barasch, A ;
Peterson, DE .
ORAL ONCOLOGY, 2003, 39 (02) :91-100
[3]   Secretion of biologically active pancreatitis-associated protein I ( PAP) by genetically modified dairy Lactococcus lactis NZ9000 in the prevention of intestinal mucositis [J].
Carvalho, Rodrigo D. ;
Breyner, Natalia ;
Menezes-Garcia, Zelia ;
Rodrigues, Nubia M. ;
Lemos, Luisa ;
Maioli, Tatiane U. ;
Souza, Danielle da Gloria ;
Carmona, Denise ;
de Faria, Ana M. C. ;
Langella, Philippe ;
Chatel, Jean-Marc ;
Bermudez-Humaran, Luis G. ;
Figueiredo, Henrique C. P. ;
Azevedo, Vasco ;
de Azevedo, Marcela S. .
MICROBIAL CELL FACTORIES, 2017, 16
[4]  
Corso G, 2016, CANC CELL MICROENVIR, V3, P1
[5]  
Erowele GI, 2009, US Pharm, V34, P10
[6]  
Gaetti-Jardim E, 2011, BRAZ J MICROBIOL, V42, P1046
[7]   Investigation of First Identified mcr-1 Gene in an Isolate from a US Patient - Pennsylvania, 2016 [J].
Kline, Kelly E. ;
Shover, Jordan ;
Kallen, Alexander J. ;
Lonsway, David R. ;
Watkins, Sharon ;
Miller, Jeffrey R. .
MMWR-MORBIDITY AND MORTALITY WEEKLY REPORT, 2016, 65 (36) :977-978
[8]   More Furious Than Ever: Escherichia coli-Acquired Co-resistance Toward Colistin and Carbapenems [J].
Kumar, Mohit ;
Saha, Sandipan ;
Subudhi, Enketeswara .
CLINICAL INFECTIOUS DISEASES, 2016, 63 (09) :1267-U144
[9]  
Lalla Rajesh V, 2008, Dent Clin North Am, V52, P61, DOI 10.1016/j.cden.2007.10.002
[10]   PerlPrimer: cross-platform, graphical primer design for standard, bisulphite and real-time PCR [J].
Marshall, OJ .
BIOINFORMATICS, 2004, 20 (15) :2471-2472